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Methods in Molecular Biology (Clifton, N.J.)
|
May 24, 2021
Fibroblast and Myofibroblast Subtypes: Single Cell Sequencing
Hesham Soliman, Lin Wei Tung, Fabio M V Rossi
Experimental Cell Research
|
November 25, 2021
Emerging skeletal muscle stromal cell diversity: Functional divergence in fibro/adipogenic progenitor and mural cell populations
Morten Ritso, Lin Wei Tung, Fabio M V Rossi
STAR Protocols
|
October 13, 2023
Protocol for generation of a time-resolved cellular interactome during tissue remodeling in adult mice
Elena Groppa, Lin Wei Tung, Stefania Mattevi, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
April 7, 2020
Murine Tissue-Resident PDGFRα+ Fibro-Adipogenic Progenitors Spontaneously Acquire Osteogenic Phenotype in an Altered Inflammatory Environment
Christine Eisner, Michael Cummings, Gabrielle Johnston, et al.
Cell Reports
|
May 21, 2026
Cachexia-induced alterations of miR-27a-3p drive cell-type specific effects in FAPs and tumor cells that coincide with muscle wasting
Ashok Narasimhan, Chun Wai Cheung, Nasim Kajabadi, et al.
Journal of Cell Science
|
August 23, 2019
Cross-talk between TGF-β and PDGFRα signaling pathways regulates the fate of stromal fibro-adipogenic progenitors
Osvaldo Contreras, Meilyn Cruz-Soca, Marine Theret, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
December 20, 2021
Cholesterol absorption blocker ezetimibe prevents muscle wasting in severe dysferlin-deficient and mdx mice
Zoe White, Marine Theret, Nadia Milad, et al.
Development (Cambridge, England)
|
March 25, 2022
Elevated numbers of infiltrating eosinophils accelerate the progression of Duchenne muscular dystrophy pathology in mdx mice
Marine Theret, Lucas Rempel, Joshua Hashimoto, et al.
Science Translational Medicine
|
June 29, 2022
Metabolic reprogramming of skeletal muscle by resident macrophages points to CSF1R inhibitors as muscular dystrophy therapeutics
Farshad Babaeijandaghi, Ryan Cheng, Nasim Kajabadi, et al.
Life Sciences
|
April 23, 2021
In vitro assessment of anti-fibrotic drug activity does not predict in vivo efficacy in murine models of Duchenne muscular dystrophy
Marine Theret, Marcela Low, Lucas Rempel, et al.
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Showing results (1-10 of 21) with videos related to
Sort By:
Page
of 3
Methods in Molecular Biology (Clifton, N.J.)
|
May 24, 2021
Fibroblast and Myofibroblast Subtypes: Single Cell Sequencing
Hesham Soliman, Lin Wei Tung, Fabio M V Rossi
Experimental Cell Research
|
November 25, 2021
Emerging skeletal muscle stromal cell diversity: Functional divergence in fibro/adipogenic progenitor and mural cell populations
Morten Ritso, Lin Wei Tung, Fabio M V Rossi
STAR Protocols
|
October 13, 2023
Protocol for generation of a time-resolved cellular interactome during tissue remodeling in adult mice
Elena Groppa, Lin Wei Tung, Stefania Mattevi, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
April 7, 2020
Murine Tissue-Resident PDGFRα+ Fibro-Adipogenic Progenitors Spontaneously Acquire Osteogenic Phenotype in an Altered Inflammatory Environment
Christine Eisner, Michael Cummings, Gabrielle Johnston, et al.
Cell Reports
|
May 21, 2026
Cachexia-induced alterations of miR-27a-3p drive cell-type specific effects in FAPs and tumor cells that coincide with muscle wasting
Ashok Narasimhan, Chun Wai Cheung, Nasim Kajabadi, et al.
Journal of Cell Science
|
August 23, 2019
Cross-talk between TGF-β and PDGFRα signaling pathways regulates the fate of stromal fibro-adipogenic progenitors
Osvaldo Contreras, Meilyn Cruz-Soca, Marine Theret, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
December 20, 2021
Cholesterol absorption blocker ezetimibe prevents muscle wasting in severe dysferlin-deficient and mdx mice
Zoe White, Marine Theret, Nadia Milad, et al.
Development (Cambridge, England)
|
March 25, 2022
Elevated numbers of infiltrating eosinophils accelerate the progression of Duchenne muscular dystrophy pathology in mdx mice
Marine Theret, Lucas Rempel, Joshua Hashimoto, et al.
Science Translational Medicine
|
June 29, 2022
Metabolic reprogramming of skeletal muscle by resident macrophages points to CSF1R inhibitors as muscular dystrophy therapeutics
Farshad Babaeijandaghi, Ryan Cheng, Nasim Kajabadi, et al.
Life Sciences
|
April 23, 2021
In vitro assessment of anti-fibrotic drug activity does not predict in vivo efficacy in murine models of Duchenne muscular dystrophy
Marine Theret, Marcela Low, Lucas Rempel, et al.
Page
of 3